1971
DOI: 10.2307/1365847
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Exploitation of Nectar Resources by Hummingbirds, Bees (Bombus), and Diglossa baritula and Its Role in the Evolution of Penstemon kunthii

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1972
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Cited by 32 publications
(19 citation statements)
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“…Schluter (1986) suggested that the bees influence nectar use by the birds and that character displacement in bird body size occurs in response to the presence or absence of bees. It has been observed a size-dependent dominance hierarchy exists among several groups of birds and insects (Brown et al, 1978;Gill & Wolf, 1979;Schaffer et al, 1979;McFarland, 1986;, where birds have negative effects on the availability of nectar to the insects (Lyon & Chadek, 1971;Primack & Howe, 1975;Boyden, 1978;Carpenter, 1979). On the other hand, insect nectarivores can also swamp the resource-defense systems of birds by sheer force of numbers (Schaffer et al, 1979;Kodric-Brown & Brown, 1979;Gill et al, 1982), as observed for honeybees in our study site.…”
Section: Temporal and Spatial Segregation Vs Territorialitysupporting
confidence: 67%
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“…Schluter (1986) suggested that the bees influence nectar use by the birds and that character displacement in bird body size occurs in response to the presence or absence of bees. It has been observed a size-dependent dominance hierarchy exists among several groups of birds and insects (Brown et al, 1978;Gill & Wolf, 1979;Schaffer et al, 1979;McFarland, 1986;, where birds have negative effects on the availability of nectar to the insects (Lyon & Chadek, 1971;Primack & Howe, 1975;Boyden, 1978;Carpenter, 1979). On the other hand, insect nectarivores can also swamp the resource-defense systems of birds by sheer force of numbers (Schaffer et al, 1979;Kodric-Brown & Brown, 1979;Gill et al, 1982), as observed for honeybees in our study site.…”
Section: Temporal and Spatial Segregation Vs Territorialitysupporting
confidence: 67%
“…Nectarivorous assemblages typically composed by either bees, hawkmoths, hummingbirds, passerine birds, and/or bats sharing resources over time, have been widely documented in the literature (Alcorn et al, 1961;Lyon & Chadek, 1971;Borrero, 1972;Primack & Howe, 1975;Cruden & Toledo, 1977;Toledo, 1977;Boyden, 1978;Des Granges, 1978;Carpenter, 1979;Feinsinger et al, 1979;, 1982Morton, 1979;Schaffer et al, 1979;Steiner, 1979;Kodric-Brown & Brown 1979;Gill et al, 1982;Kuban et al, 1983;Schluter, 1986;Eguiarte & Bú rquez, 1987;Gryj et al, 1990;Westerkamp, 1990;Sazima et al, 1993;Buzato et al, 1994;Fleming et al, 1996). Researchers have concentrated most of their attention on describing how distantly related taxa partition nectar resources and describing their role as pollinators.…”
Section: Introductionmentioning
confidence: 99%
“…), or may induce pollinators to act as secondary nectar robbers if nectar extraction is easier in robbed than in unrobbed flowers (Lara & Ornelas ; Fumero‐Cabán & Meléndez‐Ackerman ). Nectar robbers may also decrease flower nectar availability, causing a reduction in the visitation rate of pollinators (Lyon & Chadek ; Irwin & Brody ; Irwin ). A decrease or increase in legitimate visits could affect floral duration.…”
Section: Introductionmentioning
confidence: 99%
“…Documentation of food preferences (e.g., Snow 1962a, b, c, Chrome 1975) and competitive relationships (Terborgh and Diamond 1970, Leck 1971, Chrome 1975) may not provide relevant evidence because some users are not dispersers and different birds may effect dispersal in different ways (McKey 1975, Howe andEstabrook 1977). In pollination systems, different species of avian visitors have markedly different effects on plant reproduction (e.g., Lyon and Chadek 1971, Colwell 1973, Linhart 1973, Stiles 1975). Similar differences may exist among birds which ingest fruit and disperse seeds intact (Howe and Primack 1975).…”
Section: Introductionmentioning
confidence: 99%